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Volumn 72, Issue 14, 2007, Pages 908-913

New C-secosteroids from the gorgonian Tripalea clavaria

Author keywords

Gorgonian; Marine sterols; Secosteroids; Tripalea clavaria

Indexed keywords

3BETA ACETOXY 11,21,22 TRIHYDROXY 9,11 SECOCHOLEST 5 EN 9 ONE; 3BETA ACETOXY 11,22 DIHYDROXY 9,11 SECOCHOLEST 5 EN 9 ONE; 3BETA ACETOXY 11,22 DIHYDROXY 9,11 SECOERGOST 5,24(28) DIEN 9 ONE; 3BETA,11 DIHYDROXY 9,11 SECO 24 NORCHOLEST 5 EN 9 ONE; 3BETA,11,21,22 TETRAHYDROXY 9,11 SECOCHOLEST 5 EN 9 ONE; 3BETA,11,22 TRIHYDROXY 9,11 SECOCHOLEST 5 EN 9 ONE; 3BETA,11,22 TRIHYDROXY 9,11 SECOCHOLEST 5,24 DIEN 9 ONE; SECOSTEROID; UNCLASSIFIED DRUG;

EID: 35348929857     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2007.07.013     Document Type: Article
Times cited : (16)

References (25)
  • 1
    • 2942525294 scopus 로고    scopus 로고
    • New polyoxygenated steroids from the Antarctic octocoral Dasystenella acanthina
    • Mellado G.G., Zubía E., Ortega M.J., and López-González P.J. New polyoxygenated steroids from the Antarctic octocoral Dasystenella acanthina. Steroids 69 (2004) 291-299
    • (2004) Steroids , vol.69 , pp. 291-299
    • Mellado, G.G.1    Zubía, E.2    Ortega, M.J.3    López-González, P.J.4
  • 4
    • 0032862255 scopus 로고    scopus 로고
    • Steroids from sponges: recent reports
    • Aiello A., Fattorusso E., and Menna M. Steroids from sponges: recent reports. Steroids 64 (1999) 687-714
    • (1999) Steroids , vol.64 , pp. 687-714
    • Aiello, A.1    Fattorusso, E.2    Menna, M.3
  • 5
    • 0141566434 scopus 로고    scopus 로고
    • New polyhydroxy sterols: proteasome inhibitors from a marine sponge Acanthodendrilla sp.
    • Tsukamoto S., Tatsuno M., Soest R.W.M.v., Yokosawa H., and Ohta T. New polyhydroxy sterols: proteasome inhibitors from a marine sponge Acanthodendrilla sp. J Natural Prod 66 (2003) 1181-1185
    • (2003) J Natural Prod , vol.66 , pp. 1181-1185
    • Tsukamoto, S.1    Tatsuno, M.2    Soest, R.W.M.v.3    Yokosawa, H.4    Ohta, T.5
  • 6
    • 0001229636 scopus 로고
    • Polyoxygenated steroids of marine origin
    • D'Auria M.V., Minale L., and Riccio R. Polyoxygenated steroids of marine origin. Chem Rev 93 (1993) 1839-1895
    • (1993) Chem Rev , vol.93 , pp. 1839-1895
    • D'Auria, M.V.1    Minale, L.2    Riccio, R.3
  • 7
    • 9644301019 scopus 로고    scopus 로고
    • Secosteroids of marine origin
    • Sica D., and Musumeci D. Secosteroids of marine origin. Steroids 69 (2004) 743-756
    • (2004) Steroids , vol.69 , pp. 743-756
    • Sica, D.1    Musumeci, D.2
  • 8
    • 0031760606 scopus 로고    scopus 로고
    • New 9,11-secosterols from gorgonia Subergorgia suberosa of the Indian Ocean
    • Aknin M., Constantino V., Mangoni A., Fattorusso E., and Gaydou M. New 9,11-secosterols from gorgonia Subergorgia suberosa of the Indian Ocean. Steroids 63 (1998) 575-578
    • (1998) Steroids , vol.63 , pp. 575-578
    • Aknin, M.1    Constantino, V.2    Mangoni, A.3    Fattorusso, E.4    Gaydou, M.5
  • 9
    • 0030987401 scopus 로고    scopus 로고
    • Rare aromadendrane diterpenoids from a new soft coral species of Sinularia Genus of the Indian Ocean
    • Anjaneyulu A.S.R., Krishnamurthy mVR, and Rao G.V. Rare aromadendrane diterpenoids from a new soft coral species of Sinularia Genus of the Indian Ocean. Tetrahedron 53 (1997) 9301-9312
    • (1997) Tetrahedron , vol.53 , pp. 9301-9312
    • Anjaneyulu, A.S.R.1    Krishnamurthy mVR2    Rao, G.V.3
  • 10
    • 0028816876 scopus 로고
    • New antiproliferative and antiinflammatory 9,11-secosterols from the gorgonian Pseudoterogorgia sp.
    • He H., Kulanthaivel P., Baker B.J., Kalter K., Darges J., Cofield D., et al. New antiproliferative and antiinflammatory 9,11-secosterols from the gorgonian Pseudoterogorgia sp. Tetrahedron 51 (1995) 51-58
    • (1995) Tetrahedron , vol.51 , pp. 51-58
    • He, H.1    Kulanthaivel, P.2    Baker, B.J.3    Kalter, K.4    Darges, J.5    Cofield, D.6
  • 11
    • 0027481751 scopus 로고
    • New antiproliferative 9,11-secosterol from soft coral Gersemia fruticosa
    • Koljak R., Pehk T., Järving I., Liiv M., Lopp A., Varvas K., et al. New antiproliferative 9,11-secosterol from soft coral Gersemia fruticosa. Tetrahedr Lett 34 (1993) 1985-1986
    • (1993) Tetrahedr Lett , vol.34 , pp. 1985-1986
    • Koljak, R.1    Pehk, T.2    Järving, I.3    Liiv, M.4    Lopp, A.5    Varvas, K.6
  • 12
    • 35348931459 scopus 로고
    • 5-9-11-seco-gorgostene-3β, 11, 24β-triol-9-one from the gorgonian Pseudoterogorgia americana (Gmelin)
    • 5-9-11-seco-gorgostene-3β, 11, 24β-triol-9-one from the gorgonian Pseudoterogorgia americana (Gmelin). Florida Sci 53 (1990) 257-261
    • (1990) Florida Sci , vol.53 , pp. 257-261
    • Musmar, M.J.1    Weinheimer, A.J.2
  • 14
    • 33745789393 scopus 로고    scopus 로고
    • 9,11-Secosterols from the soft coral Sinularia lochmodes and Sinularia leptoclados
    • Su J.-H., Tseng Y.-J., Huang H.-H., Ahmed A.F., Lu C.-K., Wu Y.-C., et al. 9,11-Secosterols from the soft coral Sinularia lochmodes and Sinularia leptoclados. J Natural Prod 69 (2006) 850-852
    • (2006) J Natural Prod , vol.69 , pp. 850-852
    • Su, J.-H.1    Tseng, Y.-J.2    Huang, H.-H.3    Ahmed, A.F.4    Lu, C.-K.5    Wu, Y.-C.6
  • 15
    • 0026693760 scopus 로고
    • Secondary metabolites of the yellow and gray morphs of the soft coral Parerythropodium fulvum fulvum: comparative aspects
    • Green D., Kashman Y., and Benayahu Y. Secondary metabolites of the yellow and gray morphs of the soft coral Parerythropodium fulvum fulvum: comparative aspects. J Natural Prod 55 (1992) 1186-1196
    • (1992) J Natural Prod , vol.55 , pp. 1186-1196
    • Green, D.1    Kashman, Y.2    Benayahu, Y.3
  • 16
    • 0026040964 scopus 로고
    • Structure elucidation and synthesis of 3β-6α-dihydroxy-9-oxo-9,11-seco-cholest-7-en-11-al, a novel 9,11-secosterol from the sponge Spongia officinalis
    • Migliuolo A., Piccialli V., and Sica D. Structure elucidation and synthesis of 3β-6α-dihydroxy-9-oxo-9,11-seco-cholest-7-en-11-al, a novel 9,11-secosterol from the sponge Spongia officinalis. Tetrahedron 47 (1991) 7937-7950
    • (1991) Tetrahedron , vol.47 , pp. 7937-7950
    • Migliuolo, A.1    Piccialli, V.2    Sica, D.3
  • 17
    • 0028295195 scopus 로고
    • Euryspongiols: 10 new highly hydrohylated 9,11-secosteroids with antihistaminic activity from the sponge Euryspongia sp. stereochemistry and reduction
    • Dopeso J., Quiñoá E., Riguera R., Debitus C., and Bergquist P.R. Euryspongiols: 10 new highly hydrohylated 9,11-secosteroids with antihistaminic activity from the sponge Euryspongia sp. stereochemistry and reduction. Tetrahedron 50 (1994) 3813-3828
    • (1994) Tetrahedron , vol.50 , pp. 3813-3828
    • Dopeso, J.1    Quiñoá, E.2    Riguera, R.3    Debitus, C.4    Bergquist, P.R.5
  • 18
    • 0000059966 scopus 로고
    • Herbasterol, an ichthyotoxic 9,11-secosterol from the sponge Dysidea herbacea
    • Capon R.J., and Faulkner D.J. Herbasterol, an ichthyotoxic 9,11-secosterol from the sponge Dysidea herbacea. J Org Chem 50 (1985) 4771-4773
    • (1985) J Org Chem , vol.50 , pp. 4771-4773
    • Capon, R.J.1    Faulkner, D.J.2
  • 19
    • 0242624543 scopus 로고    scopus 로고
    • Aplidiasterols A and B, two new cytotoxic 9,11-secosterols from the mediterranean ascidian Aplidium conicum
    • Aiello A., Esposito G., Fattorusso E., Iuvone T., Luciano P., and Menna M. Aplidiasterols A and B, two new cytotoxic 9,11-secosterols from the mediterranean ascidian Aplidium conicum. Steroids 68 (2003) 719-723
    • (2003) Steroids , vol.68 , pp. 719-723
    • Aiello, A.1    Esposito, G.2    Fattorusso, E.3    Iuvone, T.4    Luciano, P.5    Menna, M.6
  • 20
    • 0030983738 scopus 로고    scopus 로고
    • New 26,27-cyclosterols from the Okinawan marine sponge of the Genus Xestospongia and absolute configurations of Xestokerols A and B
    • Miyaoka H., Shinohara M., Shimomura M., Mitome H., Yano A., Iguchi K., et al. New 26,27-cyclosterols from the Okinawan marine sponge of the Genus Xestospongia and absolute configurations of Xestokerols A and B. Tetrahedron 53 (1997) 5403-5412
    • (1997) Tetrahedron , vol.53 , pp. 5403-5412
    • Miyaoka, H.1    Shinohara, M.2    Shimomura, M.3    Mitome, H.4    Yano, A.5    Iguchi, K.6
  • 22
    • 0035821421 scopus 로고    scopus 로고
    • Unusual polyoxygenated sterols from a Philippines sponge Xestospongia sp.
    • Lerch M.L., and Faulkner D.J. Unusual polyoxygenated sterols from a Philippines sponge Xestospongia sp. Tetrahedron 57 (2001) 4091-4094
    • (2001) Tetrahedron , vol.57 , pp. 4091-4094
    • Lerch, M.L.1    Faulkner, D.J.2
  • 23
    • 0002035994 scopus 로고
    • Screening methods for antibacterial and antiviral agents from higher plants
    • Hostettmann K. (Ed), Academic Press, San Diego
    • Vanden Berghe D.A., and Vlietinck A.J. Screening methods for antibacterial and antiviral agents from higher plants. In: Hostettmann K. (Ed). Methods in Plant Biochemistry: Assays for Bioactivity vol. 6 (1991), Academic Press, San Diego 47-69
    • (1991) Methods in Plant Biochemistry: Assays for Bioactivity , vol.6 , pp. 47-69
    • Vanden Berghe, D.A.1    Vlietinck, A.J.2
  • 24
    • 0014951950 scopus 로고
    • Direct bioautography on thin-layer chromatograms as a method for detecting fungitoxic substances
    • Homans A.L., and Fuchs A. Direct bioautography on thin-layer chromatograms as a method for detecting fungitoxic substances. J Chromatogr 51 (1970) 327-329
    • (1970) J Chromatogr , vol.51 , pp. 327-329
    • Homans, A.L.1    Fuchs, A.2
  • 25
    • 2142858450 scopus 로고
    • High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
    • Ohtani I., Kusuni T., Kashman Y., and Kakisawa H. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids. J Am Chem Soc 113 (1991) 4092-4096
    • (1991) J Am Chem Soc , vol.113 , pp. 4092-4096
    • Ohtani, I.1    Kusuni, T.2    Kashman, Y.3    Kakisawa, H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.